Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1341026713
APP
0.925 0.080 21 25955719 missense variant G/A snv 4.0E-06 1.4E-05 3
rs529782627
APP
0.882 0.120 21 26112051 missense variant C/A snv 4.0E-06 7.0E-06 3
rs533667466
APP
0.925 0.080 21 25911912 missense variant T/C snv 3
rs63750151
APP
0.882 0.080 21 25891761 missense variant C/G;T snv 3
rs770237371
ASPSCR1
0.827 0.160 17 81996616 missense variant A/C;G snv 4.0E-06; 1.2E-05 5
rs267606673
ATP7A ; PGK1
0.776 0.240 X 78029314 missense variant C/T snv 9
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs17518584
CADM2
0.827 0.160 3 85555773 intron variant C/T snv 0.50 8
rs763872192
CD36
0.882 0.080 7 80672000 missense variant C/T snv 2.8E-05 4
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs901115236
CHCHD10 ; LOC107985577
0.882 0.120 22 23767531 missense variant G/A;T snv 1.5E-05; 1.5E-05 3
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs2337506
CHRNA7
0.925 0.080 15 32053864 intron variant A/G snv 0.60 2
rs8027814
CHRNA7
0.925 0.080 15 32058469 intron variant G/A snv 0.57 2
rs223331
CISD2
0.851 0.160 4 102872408 intron variant T/A;C snv 5
rs223330
CISD2
0.851 0.160 4 102872502 intron variant T/A;C snv 4
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs9331896
CLU ; MIR6843
0.851 0.080 8 27610169 intron variant C/G;T snv 4
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs950530102
DST
0.882 0.160 6 56704357 missense variant C/T snv 3
rs773819452
ECD
0.851 0.200 10 73160449 missense variant G/A snv 4.2E-06 4
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22